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rs794727470

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727470(C;C)
Make rs794727470(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position94414250
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs794727470
ebirs794727470
HLIrs794727470
Exacrs794727470
Varsomers794727470
Maprs794727470
PheGenIrs794727470
hapmaprs794727470
1000 genomesrs794727470
hgdprs794727470
ensemblrs794727470
gopubmedrs794727470
geneviewrs794727470
scholarrs794727470
googlers794727470
pharmgkbrs794727470
gwascentralrs794727470
openSNPrs794727470
23andMers794727470
23andMe allrs794727470
SNP Nexus

SNPshotrs794727470
SNPdbers794727470
MSV3drs794727470
GWAS Ctlgrs794727470
Max Magnitude0
ClinVar
Risk rs794727470(C;C)
Alt rs794727470(C;C)
Reference rs794727470(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL1A2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.94043562G>C
CLNSRC
CLNACC RCV000176911.1,